US4396734A - Polymer stabilizers - Google Patents

Polymer stabilizers Download PDF

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Publication number
US4396734A
US4396734A US06/245,851 US24585181A US4396734A US 4396734 A US4396734 A US 4396734A US 24585181 A US24585181 A US 24585181A US 4396734 A US4396734 A US 4396734A
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cps
ambient
composition
polymer
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US06/245,851
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Earl P. Williams
Donald H. Lorenz
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GAF Chemicals Corp
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GAF Corp
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Priority to US06/245,851 priority Critical patent/US4396734A/en
Priority to CA000396804A priority patent/CA1156775A/fr
Priority to AT82101957T priority patent/ATE14592T1/de
Priority to DE198282101957T priority patent/DE61079T1/de
Priority to DE8282101957T priority patent/DE3264996D1/de
Priority to EP82101957A priority patent/EP0061079B1/fr
Assigned to GAF CORPORATION reassignment GAF CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: LORENZ, DONALD H., WILLIAMS, EARL P.
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Publication of US4396734A publication Critical patent/US4396734A/en
Assigned to CHASE MANHATTAN BANK, THE NATIONAL ASSOCIATION reassignment CHASE MANHATTAN BANK, THE NATIONAL ASSOCIATION SECURITY INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: DORSET INC. A CORP OF DELAWARE
Assigned to GAF CHEMICALS CORPORATION reassignment GAF CHEMICALS CORPORATION CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). EFFECTIVE ON 04/11/1989 Assignors: DORSET INC.
Assigned to DORSET INC., A DE CORP. reassignment DORSET INC., A DE CORP. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). EFFECTIVE APRIL 10, 1989 Assignors: GAF CORPORATION, A DE CORP.
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/005—Stabilisers against oxidation, heat, light, ozone
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S507/00—Earth boring, well treating, and oil field chemistry
    • Y10S507/907—Indicating means, e.g. dye, fluorescing agent
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S507/00—Earth boring, well treating, and oil field chemistry
    • Y10S507/933—Acidizing or formation destroying
    • Y10S507/934—Acidizing or formation destroying with inhibitor

Definitions

  • this invention relates to novel polymer stabilizers for use in an acidic environment.
  • the invention relates to the composition of a stabilized hydrophilic or water-swellable polymer such as vinyl polymers, copolymers, interpolymers in an acid medium, which may or may not be cross-linked, to guarantee the acidic mucilages of said polymers against viscosity decrease and graining.
  • Acid solutions have long been employed in a variety of applications including acid pickling, etching, oil well rock fracturing, scale and stain removal solutions, paint strippers, metal preconditioners for painting and rust removal, etc.
  • the acid solutions generally require the addition of thickeners to improve their application and sustain their effect on the applied substrate.
  • Polymers have been recommended to provide the increased viscosity desired; however, many excellent polymer thickeners are disqualified for this application because of instability by attack of the acid on their molecular structures or by oxidative or photochemical degradation. When polymer degradation occurs, the polymeric thickener is not retained in solution and the viscosity rapidly declines.
  • polyvinyl pyrrolidone Although polyvinyl pyrrolidone is stable to acid attack, some loss of effectiveness on storage of the acidic solutions is caused by oxidative and/or photochemical degradation. Additionally, aqueous gels of polyvinyl pyrrolidone tend to become grainy on aging so that non-uniform applications of the acid medium result. Most other polymer thickeners are unstable in strong acid solution and rapidly loose thickening effectiveness over a period of several weeks to several months in storage, so that although these polymers form excellent mucilages, gels, emulsifying and suspending agents when freshly prepared, they have the disadvantage of requiring immediate use.
  • Another object is to provide a novel composition
  • a novel composition comprising an aqueous solution having a pH less than 7 and containing acid, polymeric thickener and stabilizer.
  • Still another object is to provide a stabilized vinyl polymer for use in any acidic environment.
  • the above objects are accomplished by preparing an acidic solution containing between about 0.5 and about 25 weight % of a polymer thickener and an effective quantity of the stabilizing ingredient, generally in the range of from about 0.005 to about 1 weight %, preferably from about 0.05 to about 0.75 weight %, based on the dry polymer by stirring the composition until a uniform mixture is achieved.
  • the stabilizer which is a redox indicator having from 6 to 30 carbon atoms, can be added to the mixture of polymer in the acid medium or the stabilizing agent, in the above amount, can be added directly to the dry polymer before introduction of the acidic liquid.
  • the incorporation of ingredients is generally carried out at a temperature above the freezing point of the liquid up to about 100° C. for a period of from about 1 to about 60 hours or until a homogeneous mixture is achieved, under atmospheric pressure.
  • the formulating conditions preferably employed include mixing at ambient temperature and pressure for a period of from about 4 to 50 hours.
  • the vinyl polymers of the present invention which may be employed as thickeners in acid media, are water soluble or water swellable polymers and include poly-N-vinyl-2-pyrrolidone; vinyl alkyl ether/maleic anhydride copolymers; vinyl-2-pyrrolidone/vinyl alkyl ether copolymers wherein the alkyl moiety contains from 1 to 3 carbon atoms, the lower alkyl esters of said vinyl ether/maleic anhydride copolymers, and the cross-linked polymers and interpolymers of the above.
  • the polymers of the present invention are of relatively high molecular weight.
  • the preferred polymers are homopolymers of N-vinyl-2-pyrrolidone, e.g. K 90 and K 112; and methyl vinyl ether/maleic anhydride copolymer.
  • water-soluble or water-swellable co- or ter-polymers and their esters, salts and amides are desirable viscosity stabilizers for the mucilages of the present invention.
  • These polymers may be of the block, alternating or statistical type.
  • the terpolymers may incorporate monomers having a higher molecular weight, e.g., higher alkyl vinyl ethers such as octadecyl vinyl ether, butyl vinyl ether and octyl vinyl ether monomers, provided that the amount incorporated does not destroy the water-solubility or water-swellability of the final polymer.
  • Interpolymers of this group include dicarboxylic acid anhydride and vinyl ether monomers optionally containing a cross-linking agent. Specifically indicated are the dicarboxylic acid anhydrides having the general structure: ##STR1## wherein R and R' are selected from the group consisting of hydrogen, halogen, cyano, alkyl, aryl, alkaryl, aralkyl and cycloaliphatic groups.
  • Illustrative anhydrides include maleic anhydride, chloromaleic anhydride, 2,3-dichloromaleic anhydride, 2,3-dicyano maleic anhydride, 2,3-dimethyl maleic anhydride, 2,3-diphenyl maleic anhydride, 2,3-dibenzyl maleic anhydride, 2,3-di(p-methylphenyl)maleic anhydride, 2,3-dicyclohexyl maleic anhydride, 2-methyl maleic anhydride, 2-ethyl maleic anhydride, 2-cyano maleic anhydride, 2-propyl maleic anhydride, 2-phenyl-, 2-benzyl-, 2(p-methylphenyl-) and 2-cyclohexyl-maleic anhydrides.
  • Maleic anhydride is preferred because of its ready availability and comparatively low cost.
  • the poly-basic acid moieties of the polymers of this invention are those which result from the hydrolysis of the anhydride linkage of the above an
  • the vinyl ether monomers include vinyl methyl ether, vinyl ethyl ether, vinyl propyl ether, vinyl isopropyl ether, vinyl butyl ethers, vinyl hexyl ethers, vinyl 2-ethylhexyl ethers and vinyl octyl ethers.
  • the ethers in which the alkyl group has from 1 to 4 carbon atoms are preferred.
  • the most preferred class of vinyl ethers are methyl vinyl ether, ethyl vinyl ether, propyl vinyl ethers, and the butyl vinyl ethers.
  • the third monomeric material which is optional, is a cross-linking agent which contains a plurality of polymerizable CH 2 ⁇ C ⁇ groupings and which is copolymerizable with the alpha-beta unsaturated acid anhydride and the vinyl alkyl ether monomers to form cross-linked water-swellable terpolymers.
  • Illustrative cross-linking agents include the polyunsaturated hydrocarbons such as divinyl benzene, divinyl naphthalene, divinyl cyclohexane, low molecular weight polymerized dienes such as polybutadiene and other conjugated diene polymers having substantial unsaturation remaining in the molecule; unsaturated sulfones such as hexaallyl trimethylene trisulfone; unsaturated amides such as trimethylacrylyl triazine; di- and polyunsaturated esters such as ethylene glycol diacrylate, allyl acrylate, allyl cinnamate, diallyl maleate, diallyl phthalate, diallyl malonate, etc.; polyunsaturated acids such as beta-styryl acrylic acid, etc.; polyunsaturated anhydrides such as acrylic anhydride, methacrylic anhydride, etc.; polyunsaturated ethers such as divinyl ether, diallyl
  • the preferred class of cross-linking agents are the polyunsaturated hydrocarbons, solvent soluble polymeric open-chain aliphatic conjugated dienes, and the polyalkenyl polyethers of polyalcohols containing at least 4 carbon atoms and at least 3 hydroxyl groups. All of these preferred cross-linking agents must contain a plurality of polymerizable CH 2 ⁇ C ⁇ groups, the double bond of which are not in conjugated relationship one with the other. Specific examples of the latter include polyallyl glucose, polyallyl sucrose, polyallyl levulose, polyallyl erythritol, polyallyl pentaerythritol, polyallyl sorbitol, polyallyl mannitol and the polyallyl disaccharides. The amount of cross-linking agent can vary from about 0.1% to about 10% of the combined weight of the remaining monomers.
  • Both the cross-linked and non-cross-linked polymers can be converted to partial esters, partial amides or salts by reaction with a primary or secondary alcohol, ammonia or a primary or secondary amine or an inorganic metallic alkaline material.
  • Representative alcohols are preferably aliphatic types having from 1 to about 18 carbon atoms.
  • the amines may be either aliphatic or aromatic and must have at least one replaceable hydrogen on the amine nitrogen.
  • the number of carbon atoms in the amine can vary from 1 to 18.
  • the preferred salt forming groups are those of the alkali metals.
  • the above polymers are well known and most have been added as thickeners to acid solutions for viscosity improvement therein.
  • the viscosity range of these polymers varies widely depending upon the ultimate use of the acid solution.
  • the polymer viscosity K-value varies from about 10 to 250 K, more desirably from about 15 to about 150 K.
  • polymers which can be employed in the operation of the present invention include: polyethylene oxide, polypropylene oxide, polyacrylic acid, polymethacrylic acid, sulfated polyvinyl alcohol, polystyrene sulfonate, hydrolyzed polyacrylonitrile, polyacrylamide, copolymers of maleic anhydride with styrene, isobutylene, or ethylene, copolymers of acrylic acid with N-vinylpyrrolidone and methylvinylpyridine, vinylacetate/maleic anhydride copolymers, poly(vinyl alcohol), polymers of caprolactams, e.g. poly(N-vinylcaprolactam) and their copolymers and interpolymers which comprise nylon.
  • the polymer can be in the form of a dry powder or liquid, depending upon its natural physical state.
  • the acids suitably employed to provide the acidic solutions of the present invention include mineral acids, such as hydrogen halides, phosphoric acid, nitric acid, perchloric acid, chromic acid, hypochloric acid, and sulfuric acid. Of this group, the chlorine containing acids are preferred and hydrogen chloride is most preferred.
  • Polybasic carboxylic acids, such as oxalic, tartaric, citric, adipic, fumaric, maleic and succinic acids can also be used to provide the acid media.
  • compositions of the polymer and stabilizer in the absence of an acidic solution also provides valuable compositions which may be subsequently employed in an acidic environment.
  • the compositions of the present invention need not include the acidic solution and the stabilizer can be combined with the polymer in a dry or liquid state or both components can be mixed in an inert carrier having a pH below about 7.5.
  • certain polymers e.g. methyl vinyl ether/maleic anhydride provide a hydrolyzed, acid moiety which imparts an acid character to aqueous solutions. In these cases, the separate addition of an acid is unnecessary.
  • the stabilizers of the present invention comprise a group of redox indicators having from 6 to 30 carbon atoms and containing a nitrogen radical selected from the group consisting of amino, azo and cyano; preferably having from 10 to 26 carbon atoms. These compounds retard oxidation of the polymers in an acid environment and stabilize their structures so as to minimize viscosity loss or, in some cases, increase the viscosity of an acid solution.
  • Compounds representative of this group include methylene blue, pyronine, phenosafranine, malachite green oxalate, the sodium salt of diphenylamine sulfonate, amaranth, tartrazine, methyl orange, methyl green, methyl red, neutral red; gallocyanine; o-tolidine; xylene cyanole; dimethylglyoxine; tionine; N-phenyl-1,2,4-benzenetriamine; N,N-dimethyl-p-phenylenediamine; diphenylamine; N,N-diphenylbenzidine; 3,3-dimethoxybenzidine and the dihydrochloride salt thereof; barium or sodium diphenylamine sulfonate; 1,10-phenanthroline optionally substituted with from 1 to 4 methyl or phenyl groups and the corresponding nitro, iron, sulfate, monochloride or perchlorate derivatives thereof; N-phenanthrani
  • the methylene blue; methyl-red, orange and green; pyronine Y; basic blue; neutral red; phenosafranine; malachite green oxalate; amaranth, tartrazine and sodium diphenylamine sulfonate indicators are most preferred.
  • the precise amount of stabilizer employed may vary somewhat depending on the conditions under which the polymer containing solution or mucilage is prepared. For example, when a relatively strong acid solution is employed, it is recommended that an amount above 0.05 weight % of the stabilizer based on the polymer be used in the formulation. In weaker acid solutions, containing larger amounts of polymer, as little as 0.005 weight % of the stabilizer can be used effectively.
  • stabilizers impart a color to the acid solution, which does not vary in shade or in hue as long as no polymer degradation occurs. Consequently, these stabilizers provide an additional advantage as visual stabilization indicators for the acidic compositions. This function is particularly useful when the acid solutions are to be stored over an extended period of time and for setting use dates on stored inventories.
  • the polymer Gantrez AN-119 is a copolymer of methyl vinyl ether and maleic anhydride 50/50 (K approximately 18-43).
  • Gantrez AN-169 is a similar copolymer but of higher viscosity (K approximately 84-92). Both are supplied by GAF Corporation.
  • Gantrez polymer grades AN-119 and 169 were tested at polymer concentrations of 5, 10 or 20%. It was noted that without benefit of added stabilizers, the percent decrease in viscosity is greater for the higher molecular weight polymer (169). Solutions of Gantrez AN-169, after storage for 130 days were found to retain only from 2.4 to 17.7% of their original viscosity, whereas, Gantrez AN-119 solutions retained from 60 to 69% in the same period.
  • the colors of the various Gantrez AN solutions all remained unchanged for the duration of these tests.
  • the colors formed through use of these stabilizers were as follows: malachite green-bluish green; methylene blue-blue; sodium diphenylamine sulfonate-pale yellow; pyronine Y-red; amaranth-red; tartrazine-red; phenosafranine-violet.
  • the polymer PVP-K 90 is poly(N-vinyl-2-pyrrolidone) having a viscosity K value of 90 and is supplied by GAF Corporation.
  • Example 33-54 The test procedure for Examples 33-54 was similar to that described for hydrolyzed Gantrez AN (Table 1) except that in the present examples the initial viscosity was determined after only 24 hours of slow mixing. The mixtures were mixed for another 24 hours and air bubbles rose to the surface while the mixture was allowed to stand. The viscosity was then determined using a Brookfield RVT viscometer with a No. 3 spindle at 10 or 100 RPM.
  • Examples 38 and 39 are presented to show viscosities at lower polymer concentrations in the acid solution.
  • the polymer employed in this series is poly-N-vinyl-2-pyrrolidone having a viscosity K value of 112 cross-linked with diallyl polyethylene glycol 600, (0.02 mole % cross-linked).
  • the stabilizers of the present invention demonstrate marked improvement over the prior art as represented by U.S. Pat. No. 2,894,921 which requires 3 to 120% of 8-hydroxyquinoline based on dry polymer to prevent drastic reduction in the viscosity of Gantrez solutions.
  • Stabilizers for the cross-linked polymer of Examples 55-87 were tested for one year shelf life stability of the thickened acid solution.
  • the polymer solution was prepared by mixing the stabilizer and polymer in the HCl aqueous solution in the concentration shown in Table 6.
  • Table 7 provides a guide to color changes in the stabilized acid solutions of polymer which may be expected when a decline in viscosity due to oxidation occurs.
  • the Redox indicators of the present invention have been found to aid in stabilizing acidic solutions of PVP or Gantrez AN. They retard oxidation of these polymers which results in chain scission with a decrease in viscosity or cross-linking with increased viscosity, both of which were observed in the tests conducted.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Detergent Compositions (AREA)
  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
US06/245,851 1981-03-20 1981-03-20 Polymer stabilizers Expired - Fee Related US4396734A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
US06/245,851 US4396734A (en) 1981-03-20 1981-03-20 Polymer stabilizers
CA000396804A CA1156775A (fr) 1981-03-20 1982-02-23 Stabilisateurs de polymeres
DE198282101957T DE61079T1 (de) 1981-03-20 1982-03-11 Polymerstabilisatoren.
DE8282101957T DE3264996D1 (en) 1981-03-20 1982-03-11 Polymer stabilizers
AT82101957T ATE14592T1 (de) 1981-03-20 1982-03-11 Polymerstabilisatoren.
EP82101957A EP0061079B1 (fr) 1981-03-20 1982-03-11 Stabilisateurs de polymères

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EP (1) EP0061079B1 (fr)
AT (1) ATE14592T1 (fr)
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DE (2) DE3264996D1 (fr)

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4490261A (en) * 1982-12-28 1984-12-25 Mobil Oil Corporation Acidic high temperature stable aqueous brine fluids viscosified by basic N-heterocyclic polymers
US4542175A (en) * 1979-08-23 1985-09-17 Rohm Gmbh Method for thickening aqueous systems
US4609476A (en) * 1983-05-02 1986-09-02 Mobil Oil Corporation High temperature stable aqueous brine fluids
WO1991011388A1 (fr) * 1990-02-01 1991-08-08 United States Borax & Chemical Corporation Stabilisation de solutions peroxygenees aqueuses
WO1993006165A1 (fr) * 1991-09-17 1993-04-01 Isp Investments Inc. Solution aqueuse stabilisee
US5214089A (en) * 1991-09-18 1993-05-25 Isp Investments Inc. Stabilized aqueous solution of a C1 -C5 alkyl vinyl ether and maleic acid copolymer
US5302639A (en) * 1990-10-23 1994-04-12 Shin-Etsu Chemical Co., Ltd. Polymer scale preventive agent
US5352729A (en) * 1991-11-14 1994-10-04 Basf Aktiengesellschaft Use of pigment formulations for the preparation of pastes, printing inks and coatings
US5698649A (en) * 1992-05-16 1997-12-16 Basf Aktiengesellschaft Copolymers based on vinyl ethers and monoethylenically unsaturated dicarboxylic anhydrides, their preparation and their use
US5998517A (en) * 1998-06-05 1999-12-07 Becton, Dickinson And Company Composition for the detection of microorganisms in a sample
US6008274A (en) * 1992-04-29 1999-12-28 Basf Aktiengesellschaft Stabilization of copolymers of maleic acid or maleic anhydride and vinyl alkyl ethers
US6418702B2 (en) * 1998-09-16 2002-07-16 Isp Investments Inc. Storage stabilized oxygen degradable polymer
US20030211169A1 (en) * 1998-04-30 2003-11-13 Renato Tabasso Disinfectant peracetic acid system
US20060280707A1 (en) * 2003-02-10 2006-12-14 Jong-Ho Park Composition and manufacturing method of self-diagnosis and reduction catalyst processing for permanent & straighter
US20130085090A1 (en) * 2011-09-30 2013-04-04 Samsung Electro-Mechanics Co., Ltd. Lubricating oil composition for fluid dynamic bearing and hdd motor fabricated by using the same
US20130090275A1 (en) * 2011-10-10 2013-04-11 Samsung Electro-Mechanics Co., Ltd. Lubricating oil composition for fluid dynamic bearings and hdd motor fabricated using the same
US20130090276A1 (en) * 2011-10-10 2013-04-11 Samsung Electro-Mechanics Co., Ltd. Lubricating oil composition for fluid dynamic bearing and hdd motor fabricated using the same
US20140296114A1 (en) * 2013-03-27 2014-10-02 Samsung Electro-Mechanics Co., Ltd. Lubricating oil composition for hydrodynamic bearing and hdd motor using the same

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US5298661A (en) * 1988-10-20 1994-03-29 Ricoh Company, Ltd. Charge transporting materials and electrophotographic photoconductors using the same
CN112326644B (zh) * 2020-10-29 2022-01-28 郑州大学 基于Sip-Me/DMPS可逆反应的重金属离子指示剂及应用

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US3906513A (en) * 1970-06-29 1975-09-16 Beckman Instruments Inc Low-pressure inking system
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Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4542175A (en) * 1979-08-23 1985-09-17 Rohm Gmbh Method for thickening aqueous systems
US4490261A (en) * 1982-12-28 1984-12-25 Mobil Oil Corporation Acidic high temperature stable aqueous brine fluids viscosified by basic N-heterocyclic polymers
US4609476A (en) * 1983-05-02 1986-09-02 Mobil Oil Corporation High temperature stable aqueous brine fluids
WO1991011388A1 (fr) * 1990-02-01 1991-08-08 United States Borax & Chemical Corporation Stabilisation de solutions peroxygenees aqueuses
AU637200B2 (en) * 1990-02-01 1993-05-20 United States Borax & Chemical Corp. Stabilization of aqueous peroxygen solutions
US5380456A (en) * 1990-02-01 1995-01-10 United States Borax & Chemical Corporation Stabilization of aqueous persalt solutions
US5302639A (en) * 1990-10-23 1994-04-12 Shin-Etsu Chemical Co., Ltd. Polymer scale preventive agent
AU656626B2 (en) * 1991-09-17 1995-02-09 Isp Investments Inc. Stabilized aqueous solution
WO1993006165A1 (fr) * 1991-09-17 1993-04-01 Isp Investments Inc. Solution aqueuse stabilisee
US5214089A (en) * 1991-09-18 1993-05-25 Isp Investments Inc. Stabilized aqueous solution of a C1 -C5 alkyl vinyl ether and maleic acid copolymer
US5352729A (en) * 1991-11-14 1994-10-04 Basf Aktiengesellschaft Use of pigment formulations for the preparation of pastes, printing inks and coatings
US6008274A (en) * 1992-04-29 1999-12-28 Basf Aktiengesellschaft Stabilization of copolymers of maleic acid or maleic anhydride and vinyl alkyl ethers
JP3264927B2 (ja) 1992-04-29 2002-03-11 ビーエーエスエフ アクチェンゲゼルシャフト マレイン酸または無水マレイン酸とビニルアルキルエーテルから成る共重合体を安定化させる方法
US5698649A (en) * 1992-05-16 1997-12-16 Basf Aktiengesellschaft Copolymers based on vinyl ethers and monoethylenically unsaturated dicarboxylic anhydrides, their preparation and their use
US20030211169A1 (en) * 1998-04-30 2003-11-13 Renato Tabasso Disinfectant peracetic acid system
US5998517A (en) * 1998-06-05 1999-12-07 Becton, Dickinson And Company Composition for the detection of microorganisms in a sample
US6418702B2 (en) * 1998-09-16 2002-07-16 Isp Investments Inc. Storage stabilized oxygen degradable polymer
US20060280707A1 (en) * 2003-02-10 2006-12-14 Jong-Ho Park Composition and manufacturing method of self-diagnosis and reduction catalyst processing for permanent & straighter
US20130085090A1 (en) * 2011-09-30 2013-04-04 Samsung Electro-Mechanics Co., Ltd. Lubricating oil composition for fluid dynamic bearing and hdd motor fabricated by using the same
US20130090275A1 (en) * 2011-10-10 2013-04-11 Samsung Electro-Mechanics Co., Ltd. Lubricating oil composition for fluid dynamic bearings and hdd motor fabricated using the same
US20130090276A1 (en) * 2011-10-10 2013-04-11 Samsung Electro-Mechanics Co., Ltd. Lubricating oil composition for fluid dynamic bearing and hdd motor fabricated using the same
US20140296114A1 (en) * 2013-03-27 2014-10-02 Samsung Electro-Mechanics Co., Ltd. Lubricating oil composition for hydrodynamic bearing and hdd motor using the same

Also Published As

Publication number Publication date
EP0061079B1 (fr) 1985-07-31
DE3264996D1 (en) 1985-09-05
DE61079T1 (de) 1983-04-14
EP0061079A1 (fr) 1982-09-29
CA1156775A (fr) 1983-11-08
ATE14592T1 (de) 1985-08-15

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